Long-term outcome in patients with mantle cell lymphoma following high-dose therapy and autologous stem cell transplantation.


Journal

European journal of haematology
ISSN: 1600-0609
Titre abrégé: Eur J Haematol
Pays: England
ID NLM: 8703985

Informations de publication

Date de publication:
Aug 2023
Historique:
revised: 12 04 2023
received: 07 12 2022
accepted: 14 04 2023
medline: 19 7 2023
pubmed: 25 4 2023
entrez: 24 04 2023
Statut: ppublish

Résumé

Long-term clinical and molecular remissions in patients with mantle cell lymphoma (MCL) after autologous stem cell transplantation (ASCT) have been evaluated in only a few studies. Sixty-five patients with MCL received ASCT (54 first-line ASCT, 10 second-line ASCT, and 1 third-line ASCT). In the case of long-term remission (≥5 years; n = 27), peripheral blood was tested for minimal residual disease (MRD) by t(11;14)- and IGH-PCR at the last follow-up. Ten-year overall survival (OS), progression-free survival (PFS), and freedom from progression (FFP) after first-line ASCT were 64%, 52%, and 59% versus after second-line ASCT 50%, 20%, and 20%, respectively. Five-year OS, PFS, and FFP for the first-line cohort were 79%, 63%, and 69%, respectively. Five-year OS, PFS, and FFP after second-line ASCT were 60%, 30%, and 30%, respectively. Treatment-related mortality (3 months after ASCT) was 1.5%. So far 26 patients developed sustained long-term clinical and molecular complete remissions of up to 19 years following ASCT in first treatment line. Sustained long-term clinical and molecular remissions are achievable following ASCT.

Sections du résumé

BACKGROUND BACKGROUND
Long-term clinical and molecular remissions in patients with mantle cell lymphoma (MCL) after autologous stem cell transplantation (ASCT) have been evaluated in only a few studies.
DESIGN AND METHODS METHODS
Sixty-five patients with MCL received ASCT (54 first-line ASCT, 10 second-line ASCT, and 1 third-line ASCT). In the case of long-term remission (≥5 years; n = 27), peripheral blood was tested for minimal residual disease (MRD) by t(11;14)- and IGH-PCR at the last follow-up.
RESULTS RESULTS
Ten-year overall survival (OS), progression-free survival (PFS), and freedom from progression (FFP) after first-line ASCT were 64%, 52%, and 59% versus after second-line ASCT 50%, 20%, and 20%, respectively. Five-year OS, PFS, and FFP for the first-line cohort were 79%, 63%, and 69%, respectively. Five-year OS, PFS, and FFP after second-line ASCT were 60%, 30%, and 30%, respectively. Treatment-related mortality (3 months after ASCT) was 1.5%. So far 26 patients developed sustained long-term clinical and molecular complete remissions of up to 19 years following ASCT in first treatment line.
CONCLUSION CONCLUSIONS
Sustained long-term clinical and molecular remissions are achievable following ASCT.

Identifiants

pubmed: 37094812
doi: 10.1111/ejh.13985
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

220-228

Subventions

Organisme : TRANSCAN V Novel 01KT1807 by BMBF

Informations de copyright

© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Bernd Metzner (B)

Department of Oncology and Hematology, Klinikum Oldenburg, University Clinic, Oldenburg, Germany.

Thomas H Müller (TH)

Red Cross Blood Transfusion Service NSTOB, Oldenburg, Germany.

Jochen Casper (J)

Department of Oncology and Hematology, Klinikum Oldenburg, University Clinic, Oldenburg, Germany.

Christoph Kimmich (C)

Department of Oncology and Hematology, Klinikum Oldenburg, University Clinic, Oldenburg, Germany.

Claus-Henning Köhne (CH)

Department of Oncology and Hematology, Klinikum Oldenburg, University Clinic, Oldenburg, Germany.

Eduard Petershofen (E)

Red Cross Blood Transfusion Service NSTOB, Oldenburg, Germany.

Andrea Renzelmann (A)

Department of Oncology and Hematology, Klinikum Oldenburg, University Clinic, Oldenburg, Germany.

Ruth Thole (R)

Department of Oncology and Hematology, Klinikum Oldenburg, University Clinic, Oldenburg, Germany.

Andreas Voss (A)

Department of Oncology and Hematology, Klinikum Oldenburg, University Clinic, Oldenburg, Germany.

Martin Dreyling (M)

Department of Internal Medicine III, University Hospital Munich, Grosshadern, Germany.

Eva Hoster (E)

Department of Internal Medicine III, University Hospital Munich, Grosshadern, Germany.

Wolfram Klapper (W)

Department of Pathology, Hematopathology Section and Lymph Node Registry, University of Schleswig-Holstein, Kiel, Germany.

Christiane Pott (C)

Department of Medicine II, University of Schleswig-Holstein, Kiel, Germany.

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